FDA Inspection 1003433 — Kesair Technologies, LLC

Kesair Technologies, LLC — FEI 3002959861

The FDA completed an inspection of Kesair Technologies, LLC on February 15, 2017 in Kennesaw, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 15, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Kennesaw, GA (United States)